Canonical Allele Identifier: CA2334484674
Community Standard Title: NC_000019.10:g.37256206T=
Gene: LINC01535 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.37256206T= , CM000681.2:g.37256206T= GRCh38
NC_000019.9:g.37747108T= , CM000681.1:g.37747108T= GRCh37
NC_000019.8:g.42438948T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110718.1:n.383-193T=
NR_110719.1:n.382+224T=
NR_110720.1:n.383+224T=
NR_110720.2:n.356+224T=